# Light Guide Optics International Ltd. (contract manufacturer, Livani Preilu Novads, LV): 2 new FDA device listings, incl. catheter, peripheral, atherectomy

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Light Guide Optics International Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device |
| Location | Livani Preilu Novads, LV |
| New listings | 2 |
| Devices | Catheter, Peripheral, Atherectomy; Powered Laser Surgical Instrument |
| Product codes | MCW, GEX |
| Device classes | Class II |
| Medical specialties | Cardiovascular, General, Plastic Surgery |
| Brand names | 1.5mm RX catheter (Hydrophilic); 1.5mm RX catheter (non coated); 0.9mm RX catheter (Hydrophilic); 0.9mm RX catheter (non coated); CORONA Infinite Ring XSCF 600 1.6 US; Bare Fiber 400 T Luer Lock; CORONA 360 Fused 600 1.8 US; Rigid Infinite Ring HSC Probe 600 1.8 US |
| First new listing | 2026-07-28 |
| Latest new listing | 2026-08-21 |
| FDA registration number | 3012669557 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.